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The hierarchically organized splitting of chromosome bands into sub-bands analyzed by multicolor banding (MCB)

机译:通过多色条带分析(MCB)将染色体带分层划分为子带

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摘要

To clarify the nature of chromosome sub-bands in more detail, the multicolor banding (MCB) probe-set for chromosome 5 was hybridized to normal metaphase spreads of GTG band levels at ~850, ~550, ~400 and ~300. It could be observed that as the chromosomes became shorter, more of the initial 39 MCB pseudo-colors disappeared, ending with 18 MCB pseudo-colored bands at the ~300-band level. The hierarchically organized splitting of bands into sub-bands was analyzed by comparing the disappearance or appearance of pseudo-color bands of the four different band levels. The regions to split first are telomere-near, centromere-near and in 5q23→q31, followed by 5p15, 5p14, and all GTG dark bands in 5q apart from 5q12 and 5q32 and finalized by sub-band building in 5p15.2, 5q21.2→q21.3, 5q23.1 and 5q34. The direction of band splitting towards the centromere or the telomere could be assigned to each band separately. Pseudo-colors assigned to GTG-light bands were resistant to band splitting. These observations are in concordance with the recently proposed concept of chromosome region-specific protein swelling.
机译:为了更详细地阐明染色体子带的性质,将第5号染色体的多色条带(MCB)探针与GTG带水平的正常中期扩散在850,〜550,〜400和〜300处杂交。可以观察到,随着染色体变短,最初的39个MCB伪色带消失了更多,最后在〜300波段水平上有18个MCB伪色带。通过比较四个不同波段级别的伪彩色波段的消失或外观,分析了波段分成子波段的分层组织方式。首先分裂的区域是端粒附近,着丝粒附近和5q23→q31,其次是5p15、5p14,以及5q中除5q12和5q32之外的所有GTG暗带,并通过在5p15.2、5q21中的子带构建来最终确定.2→q21.3、5q23.1和5q34。带向着着丝粒或端粒分裂的方向可以分别分配给每个带。分配给GTG轻型波段的伪色可抵抗波段分裂。这些观察结果与最近提出的染色体区域特异性蛋白溶胀的概念一致。

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